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两种单相口服避孕药的比较:孕二烯酮/炔雌醇与去氧孕烯/炔雌醇。

Comparison of two monophasic oral contraceptives: gestodene/ethinyl estradiol versus desogestrel/ethinyl estradiol.

作者信息

Benagiano G

机构信息

First Institute of Obstetrics and Gynecology, University of Rome, la Sapienza Policlinico Umberto I, Italy.

出版信息

Int J Fertil. 1989 Sep;34 Suppl:31-9.

PMID:2576255
Abstract

The contraceptive efficacy, cycle control, safety, and subject acceptance of the new contraceptive (OC) preparations containing gestodene (GTD) plus ethinyl estradiol (EE) are being compared with the combination containing desogestrel (DSG) plus EE in a randomized, open-label outpatient study. Interim data from six cycles of this ongoing study were obtained for 378 women receiving 75 micrograms GTD + 30 micrograms EE per day and 384 women receiving 150 micrograms DSG + 30 micrograms EE per day. Each group received OCs for 21 days per cycle. There were no pregnancies in subjects receiving either OC during 1,658 cycles of GTD + EE or 1,707 cycles of DSG + EE use. The continuation rates were similar in the two groups, and no major differences in type or incidence of side effects were observed. There were also no clinically significant changes in blood pressure or body weight in either group. Slightly better cycle control was observed for subjects taking GTD + EE, since the incidence of spotting and breakthrough bleeding was slightly greater for women taking DSG + EE. The incidence of amenorrhea (missed periods) tended to be lower for the subjects taking the GTD-containing preparation: 7 (0.5%) cycles compared with 12 (0.9%) DSG + EE cycles. The GTD + EE-treated subjects also had a lighter menstrual flow. Fewer subjects taking GTD + EE withdrew because of side effects typically associated with OCs. The data from this study indicate that the new combination of GTD + EE provides safe and effective oral contraception, with good tolerance and cycle control.

摘要

在一项随机、开放标签的门诊研究中,正在将含孕二烯酮(GTD)加炔雌醇(EE)的新型避孕药(OC)制剂的避孕效果、周期控制、安全性及受试者接受度与含去氧孕烯(DSG)加EE的复方制剂进行比较。从这项正在进行的研究的六个周期中获取了中期数据,这些数据来自378名每天服用75微克GTD + 30微克EE的女性和384名每天服用150微克DSG + 30微克EE的女性。每组每个周期服用OC 21天。在服用GTD + EE的1658个周期或服用DSG + EE的1707个周期中,接受任何一种OC的受试者均未怀孕。两组的持续率相似,未观察到副作用类型或发生率的重大差异。两组的血压或体重也均无临床显著变化。服用GTD + EE的受试者的周期控制略好,因为服用DSG + EE的女性点滴出血和突破性出血的发生率略高。服用含GTD制剂的受试者闭经(月经推迟)发生率往往较低:7个周期(0.5%),而服用DSG + EE的为12个周期(0.9%)。接受GTD + EE治疗的受试者月经量也较少。因OC常见副作用而退出的服用GTD + EE的受试者较少。这项研究的数据表明,GTD + EE的新复方制剂可提供安全有效的口服避孕,耐受性良好且周期控制佳。

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